17342003: Familial erythrocytosis (disorder)

SNOMED CT Concept\constatation clinique\...

\Evaluation finding\Finding of cellular component of blood (finding)\constatation à propos de la lignée rouge\Erythrocytosis\Familial erythrocytosis
\Evaluation finding\Measurement finding\Measurement finding outside reference range\Abnormal blood cell count\RBC count abnormal\Red blood cell count raised (finding)\Erythrocytosis\Familial erythrocytosis
\Evaluation finding\Measurement finding\Measurement finding outside reference range\Measurement finding above reference range\Red blood cell count raised (finding)\Erythrocytosis\Familial erythrocytosis
\Evaluation finding\Measurement finding\Red blood cell count - finding\RBC count abnormal\Red blood cell count raised (finding)\Erythrocytosis\Familial erythrocytosis
\Evaluation finding\Hematopoietic system finding\constatation à propos de la lignée rouge\Erythrocytosis\Familial erythrocytosis

\constatation à propos du sang, des lymphatiques et du système immunitaire\anomalie des éléments figurés du sang (trouble)\...

\troubles héréditaires des éléments figurés du sang\Hereditary red blood cell disorder (disorder)\Familial erythrocytosis

\anomalie de la lignée rouge\Hereditary red blood cell disorder (disorder)\Familial erythrocytosis
\anomalie de la lignée rouge\Erythrocytosis\Familial erythrocytosis

\Disease\Genetic disease\maladie héréditaire\Hereditary disorder by system\troubles héréditaires des éléments figurés du sang\Hereditary red blood cell disorder (disorder)\Familial erythrocytosis
\Disease\anomalie des éléments figurés du sang (trouble)\troubles héréditaires des éléments figurés du sang\Hereditary red blood cell disorder (disorder)\Familial erythrocytosis
\Disease\anomalie des éléments figurés du sang (trouble)\anomalie de la lignée rouge\Hereditary red blood cell disorder (disorder)\Familial erythrocytosis
\Disease\anomalie des éléments figurés du sang (trouble)\anomalie de la lignée rouge\Erythrocytosis\Familial erythrocytosis
\Disease\affection d'un système corporel\Hereditary disorder by system\troubles héréditaires des éléments figurés du sang\Hereditary red blood cell disorder (disorder)\Familial erythrocytosis
\Disease\affection d'un système corporel\anomalie de la lignée rouge\Hereditary red blood cell disorder (disorder)\Familial erythrocytosis
\Disease\affection d'un système corporel\anomalie de la lignée rouge\Erythrocytosis\Familial erythrocytosis

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Familial erythrocytosis	est un(e) (attribut)	Hereditary disorder of hematologic system	false	Inferred relationship	Some
Familial erythrocytosis	est un(e) (attribut)	Erythrocytosis	true	Inferred relationship	Some
Familial erythrocytosis	localisation d'une constatation (attribut)	structure du système hématopoïétique	false	Inferred relationship	Some
Familial erythrocytosis	est un(e) (attribut)	maladie héréditaire	false	Inferred relationship	Some
Familial erythrocytosis	est défini par la manifestation de (attribut)	Red blood cell count raised (finding)	false	Inferred relationship	Some
Familial erythrocytosis	est un(e) (attribut)	Hereditary red blood cell disorder (disorder)	true	Inferred relationship	Some
Familial erythrocytosis	localisation d'une constatation (attribut)	Erythrocyte	true	Inferred relationship	Some	2
Familial erythrocytosis	localisation d'une constatation (attribut)	structure du système hématopoïétique	false	Inferred relationship	Some
Familial erythrocytosis	a pour interprétation (attribut)	au-dessus de l'étendue de référence	true	Inferred relationship	Some	1
Familial erythrocytosis	interprète (attribut)	Haematology procedure	true	Inferred relationship	Some	3
Familial erythrocytosis	interprète (attribut)	Red blood cell count	true	Inferred relationship	Some	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Autosomal recessive secondary polycythemia not associated with Von Hippel Lindau gene (disorder)	est un(e) (attribut)	True	Familial erythrocytosis	Inferred relationship	Some
Familial erythrocytosis due to diphosphoglycerate mutase deficiency	est un(e) (attribut)	True	Familial erythrocytosis	Inferred relationship	Some
Familial polycythemia vera	est un(e) (attribut)	True	Familial erythrocytosis	Inferred relationship	Some
High oxygen affinity haemoglobin polycythaemia	est un(e) (attribut)	True	Familial erythrocytosis	Inferred relationship	Some
Chuvash erythrocytosis	est un(e) (attribut)	True	Familial erythrocytosis	Inferred relationship	Some

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
29310019	Hereditary pure erythrocytosis	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
29311015	Congenital erythrocytosis	en	Synonym (core metadata concept)	Inactive	Only initial character case insensitive (core metadata concept)	SNOMED CT core
29312010	Essential hypererythropoietinemia	en	Synonym (core metadata concept)	Inactive	Only initial character case insensitive (core metadata concept)	SNOMED CT core
29313017	Familial polycythemia	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
29314011	Erythropoietin polycythemia	en	Synonym (core metadata concept)	Inactive	Only initial character case insensitive (core metadata concept)	SNOMED CT core
29315012	Familial erythrocytosis	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
478114012	Familial polycythaemia	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
67031000077112	erythrocytose familiale	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)
689221000077119	erythrocytose familiale (trouble)	fr	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)
744529012	Familial erythrocytosis (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core